Self-management of Low Back Pain in Horticulture Workers

Sponsor
University of Florida (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06153199
Collaborator
(none)
170
1
2
62
2.7

Study Details

Study Description

Brief Summary

The primary purpose of this hybrid comparative effectiveness and implementation study is to compare two self-management strategies to manage pain, and adjust work-related ergonomic risk in nursery and landscape workers. This cluster randomized pragmatic study will compare interventions with different degrees of support and Specific aim 1 is to determine if self-management plus individualized guided participatory ergonomic choices (SM+PE) is more effective than self-management (SM) alone for improving LBP among horticulture workers. Both groups will review short self-management video modules to introduce general pain concepts and the importance of managing pain without medication, risks of opioid use, self-management of pain, and simple ergonomic strategies for both groups. Both groups will choose 1 self-management strategy to manage pain at home and 1 ergonomic workplace strategy to limit pain. The SM+PE participant's choices will be guided using branching logic questions matched to their self-identified most difficult work activities due to pain. guide choices matched to participant's most difficult work activities. This group will also: 1) review videos of their work tasks, 2) receive text reminders to support implementation, and 3) supervisors will participate in additional discussions of processes and support of workers. Surveys will include instruments reflecting low back pain disability, pain, work ability, and affective or cognitive characteristics (self-efficacy, pain anxiety, depression, coping), collected at baseline, pre- and post-intervention, with follow-ups at 3- and 6-months. Workers will be videoed pre- and post-intervention to inform simulated work analysis for calculation of work risk and to compare any changes for the most difficult tasks. Specific aim 2 will identify contextual factors impacting engagement, adoption, effectiveness, and implementation. Interviews, focus groups, and field notes will be used to explain results and establish patterns to inform future translation.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Video training - Self-management
  • Behavioral: Video training - Ergonomics
  • Behavioral: Supervisor training
  • Behavioral: Guided choice of ergonomic options matched to most difficult tasks
  • Behavioral: Prioritized lists of self management options
  • Behavioral: Text reminders
N/A

Detailed Description

Primary dependent variables will be collected at all measurement points: pain severity, interference, and persistence, pain with specific work tasks, disability, work ability, and pain medication use.71-74 Affective or cognitive characteristics potentially impacting adoption and effectiveness (secondary dependent variables or confounders) such as coping, fear, anxiety, depression, will also be collected.75-78 The post- and follow-up survey questions will also reflect adoption, opinions of interventions, effectiveness, facilitators, and barriers.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
170 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Prevention
Official Title:
Effectiveness and Implementation of Self-management Strategies for Low Back Pain Among Horticulture Workers
Anticipated Study Start Date :
Jan 15, 2024
Anticipated Primary Completion Date :
Dec 15, 2028
Anticipated Study Completion Date :
Mar 15, 2029

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Self-management

Participants will review short video modules on pain self-management without medication and ergonomic work adjustment Participants will be asked to select 1 self-management option and 1 ergonomic option to use for 10 weeks

Behavioral: Video training - Self-management
Short video modules on self-management of back pain without medication
Other Names:
  • Self-management training
  • Behavioral: Video training - Ergonomics
    Short video module on ergonomic adjustment for limiting back pain in nursery and landscape work

    Experimental: Self-management and Guided Participatory Ergonomics

    Participants will review short video modules on pain self-management without medication and ergonomic work adjustment Supervisors in these work settings will also discuss options to adjust work processes and ways to support workers implement ergonomic strategies Participants will be asked to select 1 self-management option and 1 ergonomic option to use for 10 weeks. This group will receive options guided by their self-identified most difficult work activities due to pain and options that they are not using regularly.

    Behavioral: Video training - Self-management
    Short video modules on self-management of back pain without medication
    Other Names:
  • Self-management training
  • Behavioral: Video training - Ergonomics
    Short video module on ergonomic adjustment for limiting back pain in nursery and landscape work

    Behavioral: Supervisor training
    In person discussion of work processes and support for workers to implement self-management and ergonomic modifications

    Behavioral: Guided choice of ergonomic options matched to most difficult tasks
    Survey based guidance on ergonomic choices appropriate for work tasks that are the most difficult due to back pain

    Behavioral: Prioritized lists of self management options
    Survey based guidance for prioritized choices of self-management

    Behavioral: Text reminders
    Reminders to implement choices

    Outcome Measures

    Primary Outcome Measures

    1. Roland Morris Disability Index [1 year]

      Disability Index for functional difficulties related to low back pain scored from 0-24 with low scores indicating lower disability

    2. Numeric Pain Rating Severity [1 year]

      Severity of pain reported for the past week and for the 3 most difficult work activities 0=no pain, 100=worst imaginable pain, lower scores reflect lower pain

    3. Pain Interference [1 year]

      Extent of pain interference with work activities in the past week, 0=not at all, 100=prevented working at normal level, lower scores reflect less interference

    4. Pain persistence [1 year]

      Pain in the past 3 months reported on a 5 item scale ranging from not at all to pain every day without a break.

    5. Pain impact [1 year]

      2 items with 5 point scale recording impact on work activities and social activities ranging from never to always, with lower scores reflecting less impact

    6. Pain frequency [1 year]

      Number of days in the past week pain is experienced ranging from 0-7

    7. Adoption [1 year]

      Use of the interventions reported for each work or self-management strategy selected (number of days used in the past week, how often used (never, occassionally, consistently) Higher scores and consistently are optimal

    8. Difficulty with work tasks [1 year]

      Patient Specific Functional Scale reported for 3 most difficult work activities with subscales reported on a scale of 0= no difficulty, 100=unable to perform with the average of the 3 items used for analysis.

    9. Work ability [1 year]

      Work Ability short form is reported on numeric rating scale from 0 (completely unable to work) to 10 able to work at your best

    Secondary Outcome Measures

    1. Use of medication and substances [1 year]

      Frequency of pain medication and substances for pain in past 3 months reported on a 4 item scale (never, 1-2 days, 3-4 days, 5-7 days) never is optimal. Items for alcohol, cannabis, tobacco, herbal products, acetaminophen, anti-inflammatories, muscle relaxants, opioids). Frequency of use per day on average also reported for a total estimate.

    2. Depression scale [1 year]

      Center for Epidemiology Depression Scale -Revised consists of 20 items reflecting frequency of depressive symptoms from rarely to most of the time with the total reported out of 60 with lower values as optimal

    3. Pain anxiety Symptom Scale [1 year]

      20 item instrument with the total of items reported from never to always reported out of 50. Lower values are optimal.

    4. Self-efficacy [1 year]

      PROMIS short form 8a Self-efficacy chronic disease management

    5. Self-efficacy and coping - confidence and control over pain [1 year]

      Coping Skills Questionnaire reporting confidence to be able to work and live a normal lifestyle rated on a 6 point scale from 0=not at all confident to 5=completely confident (total reported out of 10, and 7 point scale for control over pain 0=no control, 6=completely in control. The total is reported out of 12 with higher values as optimal

    6. Ergonomic risk [6 months]

      Rapid Ergonomic Behavioral Assessment rubric for video analysis with specific criteria rated out of a total of 15 indicating risk levels ranging from 1 negligible to very high

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:

    Workers

    1. working full time (30 hours or more per week) in physically demanding nursery or landscape work

    2. currently employed or self-employed in small (<20) or medium (21-40) size businesses

    3. 18 years of age or older

    4. English or Spanish speaking

    5. experiencing continuous or intermittent LBP over the past 3 months

    6. willing to be videotaped during work activities for movement analysis

    Owners, managers, supervisors

    1. Owners, managers, or supervisors who meet the same inclusion criteria as workers will be eligible to participate in the training interventions as well as the supervisory roles.

    2. All owners, managers, and supervisors who are willing to participate will be enrolled.

    Exclusion Criteria:

    Workers

    1. history of major trauma, surgery, or spinal nerve blocks in the past year

    2. seeking disability or workman's compensation

    3. self-disclosed pregnancy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Florida Gainesville Florida United States 32608

    Sponsors and Collaborators

    • University of Florida

    Investigators

    • Principal Investigator: Kim Dunleavy, PT, PhD, University of Florida

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Florida
    ClinicalTrials.gov Identifier:
    NCT06153199
    Other Study ID Numbers:
    • IRB202300756
    First Posted:
    Dec 1, 2023
    Last Update Posted:
    Dec 1, 2023
    Last Verified:
    Nov 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 1, 2023